中国临床解剖学杂志 ›› 2019, Vol. 37 ›› Issue (6): 644-649.doi: 10.13418/j.issn.1001-165x.2019.06.008

• 实验研究 • 上一篇    下一篇

杜仲绿原酸通过PI3K/AKT/Nrf-2通路增强视网膜母细胞瘤细胞系HXO-Rb44放射敏感性

刘铭1, 王俊2, 李丽2, 成仲夏1   

  1. 1.成都大学附属医院眼科,  成都   610081;    2.四川省人民医院眼科,  成都   610072
  • 收稿日期:2019-03-11 出版日期:2019-11-25 发布日期:2019-12-02
  • 作者简介:刘铭(1980-),女,副主任医师,研究方向:眼科临床,E-mail:liuming1980922@163.com
  • 基金资助:
    四川省卫计委科研项目(18PJ150)

Eucommia chlorogenic acid enhances the radiosensitivity of retinoblastoma cell line HXO-Rb44 via PI3K/AKT/Nrf-2 pathway

LIU Ming1, WANG Jun 2, LI Li2, CHENG Zhong-xia1   

  1. 1. Department of Ophthalmology, Affiliated Hospital of Chengdu University, Chengdu 610081; 2. Department of Ophthalmology, Sichuan Provincial People's Hospital, Chengdu 610072, China
  • Received:2019-03-11 Online:2019-11-25 Published:2019-12-02

摘要: 目的 探究杜仲绿原酸(CGA)通过调控PI3K/AKT/Nrf-2通路,对视网膜母细胞瘤细胞系HXO-Rb44放射敏感性的增强作用。  方法 通过不同浓度的CGA处理HXO-Rb44细胞,检测IC10,作为后续实验中CGA浓度。将细胞分为Ctrl、Radio、CGA、Radio+CGA组,Radio组给予4 MV X射线照射24 h,CGA组使用CGA处理24 h,Radio+CGA组在CGA处理24 h后再给予4 MV X射线照射24 h,流式细胞术检测细胞周期与细胞凋亡,蛋白质印迹检测Ki67、依赖还原型辅酶I/II醌氧化还原酶I(NQO1)、活化型半胱天冬酶(cl-caspase-3)、硫氧还蛋白还原酶1(TrxR1)、活化磷脂酰肌醇3-激酶(p-PI3K)、蛋白激酶B(AKT)、p-AKT、核因子E2相关因子2(Nrf2)蛋白表达。进一步通过PI3K激活剂740Y-P处理细胞,检测细胞周期、凋亡、增殖和相关蛋白表达、PI3K/AKT/Nrf2通路蛋白表达。  结果 随着CGA浓度的增高,细胞的相对存活率降低,药物毒性呈浓度依赖性,IC10为81.59 μmol/L。与Ctrl组相比,Radio和CGA组G2/M期细胞比例显著升高,细胞凋亡比率显著升高(P<0.01);与Radio组相比,Radio+CGA组G2/M期细胞比例和细胞凋亡比率进一步显著升高(P<0.01)。同时在蛋白水平上,与Ctrl组相比,Radio和CGA组Ki67、NQO1、TrxR1、p-PI3K、Nrf2蛋白表达及p-AKT/AKT比率显著降低(P<0.01);放射和CGA联合作用进一步降低以上各指标(P<0.01)。此外,PI3K激活剂可逆转放射对细胞周期、增殖、凋亡以及PI3K/AKT/Nrf2通路的作用,CGA可恢复放射引起的上述各指标的变化(P<0.01)。  结论 CGA可增强HXO-Rb44细胞的放射敏感性,其作用机制与抑制PI3K/AKT/Nrf2通路相关。

关键词: 杜仲绿原酸,  放射敏感性,  视网膜母细胞瘤,  PI3K/AKT/Nrf2通路

Abstract: Objective To investigate the enhancement of eucommia chlorogenic acid(CGA) on the radiosensitivity of retinoblastoma cell line HXO-Rb44 by regulating PI3K/AKT/Nrf-2 pathway.  Methods  HXO-Rb44 cells were treated with different concentrations of CGA, then IC10 was detected as CGA concentration in subsequent experiments. Cells were divided into 4 groups: a Ctrl group, a Radio group, a CGA group and a Radio+CGA group. Radio group was  disposed with 4 MV X-rays for 24 h, CGA group was processed with CGA for 24 h, and Radio+CGA group was disposed with 4 MV X-rays for 24 h after CGA treatment for 24 h. Flow cytometry was used to detect the cell cycle and cell apoptosis. The protein expressions of Ki67, NAD (P) H quinone oxidoreductase I (NQO1), cleaved-caspase-3 (cl-caspase-3), thioredoxin reductase-1 (TrxR1), activated phosphatidylinositol 3-kinase (PI3K), protein kinase B (AKT), p-AKT and nuclear factor-erythroid 2-related factor 2 (Nrf2) were determined by Western blot. Furthermore, PI3K activator 740Y-P was added to detect, the cell cycle, cell apoptosis, cell proliferation and apoptosis associated protein expressions, expressions of proteins in PI3K/AKT/Nrf2 pathway.   Results   With the increasing concentrations of CGA, the relative survival rates of cells were decreased, and the drug toxicity was concentration-dependent. The IC10 value was 81.59 μmol/L. Compared with Ctrl group, the cell population in G2/M period was significantly increased, and the cell apoptosis rates were increased in Radio group and CGA group (P<0.01). Compared with Radio group, the cell population in G2/M period and cell apoptosis rates were increased further in Radio+CGA group. Meanwhile, compared with Ctrl group, the protein expressions of Ki67, NQO1, TrxR1, p-PI3K, Nrf2 and p-AKT/AKT ratios in other groups were decreased significantly (P<0.01),  and the combined effect of Radiation and CGA further reduced the above indicators in Radio+CGA group. Furthermore, PI3K activator could reverse the effects of radiation treatment on cell cycle, cell proliferation, cell apoptosis and PI3K/AKT/Nrf2 pathway. CGA could restore the changes of the above indicators caused by radiation (P<0.01).   Conclusions   CGA can enhance the radiosensitivity of retinoblastoma cell line HXO-Rb44, and  the protective effect of CGA may be related to its inhibition of PI3K/AKT/Nrf2 pathway.

Key words: Eucommia chlorogenic acid; ,  , Radiosensitivity; ,  , Retinoblastoma; ,  , PI3K/AKT/Nrf2 pathway

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